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病例报告:行为变异型额颞叶痴呆中的紧张性木僵

Case Report: Catatonic Stupor in Behavioral Variant Frontotemporal Dementia.

作者信息

de França Gustavo Campos, Barreto Henrique Carneiro de Barros, Paranhos Thiago, Nunes Julio Cesar, de Oliveira-Souza Ricardo

机构信息

The D'Or Institute for Research and Education, Rio de Janeiro, Brazil.

The Federal University of the State of Rio de Janeiro, Gaffrée e Guinle Hospital, Rio de Janeiro, Brazil.

出版信息

Front Neurol. 2022 Jan 18;12:798264. doi: 10.3389/fneur.2021.798264. eCollection 2021.

DOI:10.3389/fneur.2021.798264
PMID:35115996
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8805594/
Abstract

Catatonia is a psychomotor syndrome common to several medical and neuropsychiatric disorders. Here, we report on the case of a 95-year-old woman who underwent a radical change in personality characterized by sexual disinhibition, and physical and verbal aggressiveness. Over several months, she developed verbal stereotypies, gait deterioration, and double incontinence. She eventually developed mutism and an active opposition to all attempts to be fed or cared for. Benzodiazepines, olanzapine and electroconvulsive therapy were of no benefit. Magnetic resonance imaging revealed asymmetric (more severe on the right) frontotemporal, parietal, and upper brainstem atrophy. She died from sepsis without recovering from stupor seven years after the onset of symptoms. We believe that the initial behavioral disinhibition was related to the frontotemporal injury, whereas catatonic stupor reflected the progression of the degenerative process to the parietal cortices. Our case adds to the small number of cases of catatonia as a symptom of degenerative dementia. It also supports the idea that damage to the parietal cortex gives rise to pathological avoidance of which catatonic stupor represents an extreme form.

摘要

紧张症是一种常见于多种医学和神经精神疾病的精神运动综合征。在此,我们报告一例95岁女性病例,其性格发生了根本性变化,表现为性抑制解除、身体和言语攻击性。在几个月的时间里,她出现了言语刻板行为、步态恶化和大小便失禁。最终,她发展为缄默症,并积极抗拒所有喂食或护理尝试。苯二氮䓬类药物、奥氮平和电休克治疗均无效。磁共振成像显示不对称(右侧更严重)的额颞叶、顶叶和上脑干萎缩。症状出现七年后,她死于败血症,昏迷状态未恢复。我们认为最初的行为抑制与额颞叶损伤有关,而紧张性木僵反映了退行性过程向顶叶皮质的进展。我们的病例增加了作为退行性痴呆症状的紧张症的少数病例。它还支持这样一种观点,即顶叶皮质损伤会导致病理性回避,而紧张性木僵是其极端形式。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c8ad/8805594/9754831c5e61/fneur-12-798264-g0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c8ad/8805594/9cc60bfb6368/fneur-12-798264-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c8ad/8805594/a87701b1565b/fneur-12-798264-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c8ad/8805594/9754831c5e61/fneur-12-798264-g0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c8ad/8805594/9cc60bfb6368/fneur-12-798264-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c8ad/8805594/a87701b1565b/fneur-12-798264-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c8ad/8805594/9754831c5e61/fneur-12-798264-g0003.jpg

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本文引用的文献

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Catatonia as the Initial Manifestation of Dementia with Lewy Bodies.以锥体外系症状为初始表现的路易体痴呆
Am J Case Rep. 2021 Jul 7;22:e932018. doi: 10.12659/AJCR.932018.
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Catatonia as Presenting Manifestation of Behavioral Frontotemporal Dementia: Insight From a PET/MRI Study.紧张症作为行为性额颞叶痴呆的首发表现:一项PET/MRI研究的见解
Prim Care Companion CNS Disord. 2021 Apr 15;23(2):20l02754. doi: 10.4088/PCC.20l02754.
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Brainstem alterations contribute to catatonia in schizophrenia spectrum disorders.脑干改变与精神分裂症谱系障碍的紧张症有关。
Schizophr Res. 2020 Oct;224:82-87. doi: 10.1016/j.schres.2020.09.025. Epub 2020 Oct 9.
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Treatment of Catatonia in Frontotemporal Dementia: A Lesson From Zolpidem Test.额颞叶痴呆中紧张症的治疗:来自唑吡坦试验的经验教训。
Clin Neuropharmacol. 2019 Sep/Oct;42(5):186-187. doi: 10.1097/WNF.0000000000000362.
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Heterogeneity in the psychiatric presentation of behavioural variant frontotemporal dementia (bvFTD).行为变异型额颞叶痴呆(bvFTD)精神症状表现的异质性。
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Structure and neural mechanisms of catatonia.紧张症的结构与神经机制
Lancet Psychiatry. 2019 Jul;6(7):610-619. doi: 10.1016/S2215-0366(18)30474-7. Epub 2019 Jun 10.
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Cortical Contributions to Distinct Symptom Dimensions of Catatonia.皮质对紧张症不同症状维度的贡献。
Schizophr Bull. 2019 Oct 24;45(6):1184-1194. doi: 10.1093/schbul/sby192.
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FTD with catatonia-like signs that temporarily resolved with zolpidem.伴有类紧张症体征的额颞叶痴呆,使用唑吡坦后暂时缓解。
Neurol Clin Pract. 2013 Aug;3(4):354-357. doi: 10.1212/CPJ.0b013e318296f263.
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